跳轉至內容
Merck
全部照片(1)

重要文件

E8034

Sigma-Aldrich

Monoclonal Anti-EEA1 antibody produced in mouse

~1.0 mg/mL, clone EEA1-C33, purified immunoglobulin, buffered aqueous solution

同義詞:

Anti-Early endosomal antigen 1, Anti-MST105, Anti-MSTP105, Anti-ZFYVE2

登入查看組織和合約定價


About This Item

分類程式碼代碼:
12352203
暫時無法取得訂價和供貨情況

生物源

mouse

共軛

unconjugated

抗體表格

purified immunoglobulin

抗體產品種類

primary antibodies

無性繁殖

EEA1-C33, monoclonal

形狀

buffered aqueous solution

分子量

antigen ~160 kDa

物種活性

human, mouse, rat

濃度

~1.0 mg/mL

技術

western blot: 2-4 μg/mL using whole extract of rat NRK or human HeLa cells

同型

IgG1

UniProt登錄號

運輸包裝

dry ice

儲存溫度

−20°C

目標翻譯後修改

unmodified

基因資訊

human ... EEA1(8411)
mouse ... Eea1(216238)
rat ... Eea1(314764)

一般說明

The gene Early Endosome Antigen 1 (EEA1) encodes for around 1400 amino acid proteins. It is a peripheral membrane protein associated with the cytoplasmic face of early endosomes. EEA1 is a autoantigen associated with subacute cutaneous systemic lupus erythematosus and is a coiled-coil protein localized to early endosomes and cytosol.

應用

Monoclonal Anti-EEA1 antibody produced in mouse is suitable for the following applications:
  • Western blotting (at a concentration of 2-4μg/mL using whole extract of rat NRK or human HeLa cells)
  • Immunofluorescence Analysis
  • Immunocytochemistry

生化/生理作用

Early Endosome Antigen 1 (EEA1) controls vesicle fusion during endocytosis. In neurons, it is involved in recycling of synaptic vesicles and neurotransmitter receptors. Patients with neurological deficits develop EEA1 autoantibodies. Mutation in EEA1 gene leads to susceptibility to diabetes in the Japanese population. Phosphatidylinositol 3-phosphate (PtdIns(3)P) is essential for the localization and function of EEA1.

外觀

0.01M 磷酸缓冲盐溶液,pH 7.4,含 15mM 叠氮化钠。

免責聲明

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

未找到適合的產品?  

試用我們的產品選擇工具.


從最近期的版本中選擇一個:

分析證明 (COA)

Lot/Batch Number

未看到正確版本?

如果您需要一個特定的版本,您可以透過批號來尋找特定憑證。

已經擁有該產品?

您可以在文件庫中找到最近購買的產品相關文件。

存取文件庫

Chae-ryun Yi et al.
Journal of virology, 82(11), 5307-5315 (2008-03-28)
Abelson murine leukemia virus (Ab-MLV) arose from a recombination between gag sequences in Moloney MLV (Mo-MLV) and the c-abl proto-oncogene. The v-Abl oncoprotein encoded by Ab-MLV contains MA, p12, and a portion of CA sequences derived from the gag gene
Christoph Kaether et al.
Traffic (Copenhagen, Denmark), 7(4), 408-415 (2006-03-16)
Alzheimer's disease is characterized by brain deposition of extracellular amyloid beta-peptide (Abeta)-containing plaques. The cellular site of gamma-secretase activity, which releases Abeta and the corresponding amyloid precursor protein intracellular domain (AICD), remains controversial. Proposed cleavage sites range from the endoplasmic
Annalisa Carlucci et al.
The Journal of biological chemistry, 285(50), 39260-39270 (2010-10-07)
PTPD1, a cytosolic non-receptor protein-tyrosine phosphatase, stimulates the Src-EGF transduction pathway. Localization of PTPD1 at actin cytoskeleton and adhesion sites is required for cell scattering and migration. Here, we show that during EGF stimulation, PTPD1 is rapidly recruited to endocytic
Mafalda Lopes da Silva et al.
Traffic (Copenhagen, Denmark), 13(10), 1351-1363 (2012-07-12)
The obligate intracellular liver stage of the Plasmodium parasite represents a bottleneck in the parasite life cycle and remains a promising target for therapeutic intervention. During this stage, parasites undergo dramatic morphological changes and achieve one of the fastest replication
Teddy Grand et al.
Kidney international, 76(9), 999-1005 (2009-08-07)
Dent's disease is an X-linked recessive disorder affecting the proximal tubules and is frequently associated with mutations in CLCN5, which encodes the electrogenic chloride-proton exchanger ClC-5. To better understand the functional consequences of CLCN5 mutations in this disease, we screened

Questions

Reviews

No rating value

Active Filters

我們的科學家團隊在所有研究領域都有豐富的經驗,包括生命科學、材料科學、化學合成、色譜、分析等.

聯絡技術服務